| 영문 | abnormality, anomaly | 한글 | 이상, 비정상 |
|---|---|---|---|
| 설명 | 정상을 벗어난 성질 혹은 사실. anomaly, aberration 등도 이상 상태를 나타내는 것이지만 abnormality가 가장 넓은 의미의 이상이다. anomaly는 보통 선천적 이상을 의미하며, aberration은 맨 눈으로 보이지 않는 이상을 의미하는 경우가 많다. |
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| 영문 | uterine tube | 한글 | 난관, 자궁관 |
|---|---|---|---|
| 설명 | 난소와 자궁을 연결하는 관. 이곳을 통해 난자가 자궁으로 운반된다. 또한 수정된 수정란이 자궁외에 착상하는 자궁외임신이 가장 많이 발생하는 장소이다. |
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| 영문 | uterine tube, salpinx | 한글 | 자궁관 |
|---|---|---|---|
| 설명 | 1. 난소와 자궁을 연결하는 관. 이곳을 통해 난자가 자궁으로 운반된다. 또한 수정된 수정란이 자궁외에 착상하는 자궁외임신이 가장 많이 발생하는 장소이다. 2. 좁은 의미로 귀인두관과 자궁관을 지칭한다. |
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| 영문 | uterine myoma | 한글 | 자궁근종 |
|---|---|---|---|
| 설명 | 보통 20대, 30대에 많다. 자궁근육층 내에 경계가 명료하고 피막을 갖지 않는 회백색의 종괴로서, 보통원형으로 단단하고 절단면에 나선형 무늬가 보인다. 평활근으로 되어 있으며, 자궁근육층내, 자궁강내 혹은 자궁밖으로 성장한다. |
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| HIVD | Herniation(Herniated) of Inter-Vertebral Disc - Cervical HIVD &... |
|---|---|
| JVP | [POMD P 49 - 52] 1) Jugular Vein Pressure 2) Jugular Venous Pulse ... |
| TOF | 1) Tetralogy Of Fallot ? CIx of Corrective Op ... |
| BCA | balloon catheter angioplasty; bicinchoninic acid; blood color analyzer; Blue Cross Association; bran... |
| CHIME | coloboma, heart anomaly, ichthyosis, mental retardation, ear abnormality |
| SAA | South Atlantic Anomaly |
|---|---|
| MCA | multiple congenital anomaly |
| AUB | Abnormal Uterine Bleeding |
| DUB | Dysfunctional uterine bleeding |
| IUCD | Intra Uterine Contraceptive Device |
| uterine opening of uterine tubes | The uterine opening of the oviduct. Synonym: ostium uterinum tubae, ostium internum, uterine opening of uterine tubes. (05 Mar 2000) |
|---|---|
| uterine ostium of uterine tubes | The uterine opening of the oviduct. Synonym: ostium uterinum tubae, ostium internum, uterine opening of uterine tubes. (05 Mar 2000) |
| uterine part of uterine tube | The part of the uterine tube located within the wall of the uterus. Synonym: pars uterina tubae uterinae. (05 Mar 2000) |
| Alder's anomaly | Coarse azurophilic granulation of leukocytes, especially granulocytes, which may be associated with gargoylism and Morquio's disease. (05 Mar 2000) |
| angle of anomaly | <ophthalmology> An obsolete term for the degree of deviation from parallelism of the visual axes of the eyes. (05 Mar 2000) |
| anomaly | A marked deviation from the normal standard, especially as a result of congenital defects. Origin: Gr. Anomalia (18 Nov 1997) |
| Aristotle's anomaly | When a small object is held between the first and second fingers crossed in such a way that it touches or presses upon skin surfaces which ordinarily are not pressed upon simultaneously by a single object, it is perceived falsely as two. (05 Mar 2000) |
| May-Hegglin anomaly | A disorder in which neutrophils and eosinophils contain basophilic structures known as Dohle or Amato bodies and in which there is faulty maturation of platelets, with thrombocytopenia; autosomal dominant inheritance. Synonym: May-Hegglin anomaly. (05 Mar 2000) |
| pelger-huet anomaly | An inherited defect interfering with normal nuclear lobulation of neutrophils and eosinophils. The nuclei appear rodlike, spherical, or dumbbell-shaped and their structure is coarse and lumpy. (12 Dec 1998) |
| Pelger-Huet nuclear anomaly | Congenital inhibition of lobulation in the nuclei of neutrophilic leukocytes; most cells present band or bilobulate appearance, and only an occasional cell is trilobed; it is not associated with disease, but may be confused with leukocyte "shift to left"; autosomal dominant inheritance. (05 Mar 2000) |
| Chediak-Steinbrinck-Higashi anomaly | <syndrome> An autosomal recessive disorder characterised by the presence of giant lysosomal vesicles in phagocytes and in consequence poor bactericidal function due to deficient secretion of myeloperoxidase by lysosomes. There is some perturbation of microtubule dynamics. There are abnormalities of granulation and nuclear structure of all types of leukocytes with malformation of peroxidase-positive granules, cytoplasmic inclusions, and Dohle bodies, often with hepatosplenomegaly, lymphadenopathy, anaemia, thrombocytopenia, roentgenologic changes of bones, lungs and heart, skin and psychomotor abnormalities, and susceptibility to infection. The condition usually results in death in childhood, before the age of 10. Reported from humans, albino Hereford cattle, mink, beige mice and killer whale. Compare: chronic granulomatous disease. Inheritance: autosomal recessive. Synonym: Beguez Cesar disease, Chediak-Higashi disease, Chediak-Steinbrinck-Higashi anomaly. (21 May 1997) |
| Rieger's anomaly | Mesodermal dysgenesis of cornea and iris, producing pupillary anomalies, posterior embryotoxon, and secondary glaucoma. Synonym: Rieger's anomaly. (05 Mar 2000) |
| Peters' anomaly | <syndrome> A congenital disorder originating from faulty separation of embryonic structures; it results in bilateral central corneal opacities, with an anterior ring attachment of the iridic pupillary border and anterior polar cataracts; associated with short-limbed dwarfism; autosomal dominant inheritance. See: iridocorneal endothelial syndrome. Synonym: Peters' anomaly. (05 Mar 2000) |
| morning glory anomaly | <ophthalmology, syndrome> A congenital anomaly of the optic disk in which there is a funnel-shaped hypoplastic optic nerve, which has a dot of white tissue at the centre, surrounded by an elevated anulus of chorioretinal pigment. The retinal vessels seen are multiple narrow bands at the edge of the disk. (22 Sep 2002) |
| Hegglin's anomaly | A disorder in which neutrophils and eosinophils contain basophilic structures known as Dohle or Amato bodies and in which there is faulty maturation of platelets, with thrombocytopenia; autosomal dominant inheritance. Synonym: May-Hegglin anomaly. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|